A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5987090



Internal ID21896433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:199608077..199608849hg38UCSC Ensembl
chr2:200472800..200473572hg19UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg38773
hg19773
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17519742
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5987090
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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